Canonical Allele Identifier: PA2825128254
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 925496

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly69Asp
CA059672
NM_000335.5:c.206G>A